The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126180771 12618077 1 I 20160720 20160720 20160803 20160803 PER US-JNJFOC-20160717715 JANSSEN 77.00 YR E M Y 95.26000 KG 20160803 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126180771 12618077 1 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 42601978 0 10 MG ORODISPERSIBLE TABLET
126180771 12618077 2 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 42601978 22578 10 MG ORODISPERSIBLE TABLET
126180771 12618077 3 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 42601978 22578 10 MG ORODISPERSIBLE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126180771 12618077 1 Urticaria
126180771 12618077 2 Pruritus
126180771 12618077 3 Food allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126180771 12618077 Drug administration error
126180771 12618077 Off label use
126180771 12618077 Product use issue
126180771 12618077 Therapeutic response unexpected

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126180771 12618077 1 20160720 20160720 0
126180771 12618077 2 20160720 20160720 0
126180771 12618077 3 20160720 20160720 0